CN1195284A - Gels with antimicrobial physical activity for cosmetics - Google Patents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/345—Alcohols containing more than one hydroxy group
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- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/042—Gels
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8147—Homopolymers or copolymers of acids; Metal or ammonium salts thereof, e.g. crotonic acid, (meth)acrylic acid; Compositions of derivatives of such polymers
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/005—Antimicrobial preparations
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/52—Stabilizers
- A61K2800/524—Preservatives
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Abstract
一种凝胶,它在所得产品中的比例为20%,其中包含至少一种多元醇、至少一种(甲基)丙烯酸聚合物和至少一种如通式所示的液化溶剂,R1-O-(R2-O-R2)n-OR3其中R1是氢原子或C1-C5直链或支链烷基,R2是C1-C5直链或支链烷基,R3是氢原子或C1-C5直链或支链烷基,n是1—200000的整数。A gel comprising 20% of the resulting product comprising at least one polyol, at least one (meth)acrylic polymer and at least one liquefying solvent of the general formula, R 1 - O-(R 2 -O-R 2 ) n -OR 3 where R 1 is hydrogen atom or C 1 -C 5 straight or branched chain alkyl, R 2 is C 1 -C 5 straight or branched chain alkyl , R 3 is a hydrogen atom or a C 1 -C 5 linear or branched alkyl group, and n is an integer ranging from 1 to 200,000.
Description
本发明涉及用于化妆品或皮肤用药的具有抗微生物物理活性的凝胶。The present invention relates to a gel with antimicrobial physical activity for cosmetic or dermatological use.
多数适用于局部涂敷的化妆品或皮肤用药品,无论它们属于哪种盖伦制剂:水包油型乳化体、油包水型乳化体、乳液、洗剂、凝胶、溶液,都包含一种或多种抗微生物物质。原因很明显:用于制备这些产品的原料很少经完全灭菌处理,所得的产品(含香精、生物活性化合物、维生素)很难继续保持灭菌状态。因此需要防止产品被不利于使用者健康或不利于产品美观的微生物污染。在生产过程中(包括所采用的原料)、包装时未经密封、以及尤其是在开盖使用后与环境接触或与使用者本身接触均会造成污染。Most cosmetic or dermatological products suitable for topical application, regardless of their galenical form: oil-in-water emulsions, water-in-oil emulsions, lotions, lotions, gels, solutions, contain a or multiple antimicrobial substances. The reason is obvious: the raw materials used to prepare these products are rarely fully sterilized, and the resulting products (including fragrances, bioactive compounds, vitamins) are difficult to maintain in a sterile state. There is therefore a need to prevent contamination of the product with microorganisms which are detrimental to the health of the user or to the aesthetics of the product. During the production process (including the raw materials used), unsealed packaging, and especially contact with the environment or the user after opening and using will cause pollution.
与食品或药品相反,化妆品无需标注有效期;因此它们能够而且应当长期保持稳定并处于最佳状态(包括其微生物状态)。In contrast to food or pharmaceuticals, cosmetics do not need to be labeled with an expiration date; they can and should therefore remain stable and in optimal condition (including their microbiological status) over the long term.
可在这类产品中采用化学防腐剂来达到该防护作用。欧洲、美洲和亚洲的各种不同法规对所用的抗微生物物质或杀菌剂分子的选择进行了严格限制。Chemical preservatives can be used in such products to achieve this protection. Various regulations in Europe, the Americas and Asia place strict restrictions on the choice of antimicrobial or fungicide molecules used.
为了产生效用,所有的防腐剂都应具有化学活性,能破坏微生物细胞的细胞壁或生化机制,因此难怪有时与这些杀菌剂分子本身接触时,它们对人体细胞也会有损害作用。实际上,随着化妆品和皮肤用药品消费量的增长,对这些产品的耐受不良的情况(刺激性、过敏)也平行增长。不同的皮肤学家、药物学家或健康权威的研究表明:某些事故是由这些产品中所含的防腐剂引起的。To be effective, all preservatives should be chemically active, disrupting the cell walls or biochemical mechanisms of microbial cells, so it is no wonder that these microbicide molecules are sometimes damaging to human cells when in contact with them themselves. In fact, as the consumption of cosmetic and dermopharmaceuticals increases, the cases of intolerances (irritants, allergies) to these products grow in parallel. Studies by various dermatologists, pharmacologists or health authorities have shown that some accidents are caused by the preservatives contained in these products.
另外,我们所处的时代的生态趋势强调化妆品工业应提供“天然”、“温和”或“低刺激性”的产品。人们在寻求一种无需加入防腐剂而对膏霜进行防护的方法。In addition, the ecological trends of our time emphasize that the cosmetic industry should offer "natural", "mild" or "low-irritant" products. People are looking for a way to protect creams without adding preservatives.
但配制不合防腐剂的化妆品并不容易。目前可选取采用灭菌的原料,并确保在严格的无菌卫生条件下进行生产(在灭菌容器中经层流处理)。但在使用中仍存在被污染的危险。只有选择特殊的包装,确保在使用时每次取出适用剂量,并能防止空气和细菌进入容器内,这样才能满足上述条件。But formulating paraben-free cosmetics is not easy. At present, sterilized raw materials can be selected and produced under strict aseptic and hygienic conditions (laminar flow treatment in a sterilized container). However, there is still a risk of contamination during use. The above conditions can only be met by choosing special packaging that ensures that the appropriate dose is taken out each time it is used, and that prevents air and bacteria from entering the container.
因此,可制成的不含防腐剂的化妆品的种类是有限的,尤其是其生产、加工和包装成本会显著增加。Therefore, the kinds of preservative-free cosmetics that can be made are limited, especially the production, processing and packaging costs will increase significantly.
法国专利2682296提出了一种非化学防腐方法,其主要特征是采用甘油基聚(甲基)丙烯酸酯类凝胶,其特点是对环境具有较强的渗透作用,从而通过失水使化妆品制剂内的微生物失活。微生物过污染试验(例如,在含40%所讨论的凝胶而不含化学防腐剂的膏霜上,每克膏霜接种106个细菌,仅在制剂中有凝胶存在的条件下控制接种7天)能说明该凝胶的抗微生物功效。已证明该专利中描述的方法是可实施的,但存在一些缺点:化妆品组合物所需的凝胶数量很高(最佳情况下至少是40%;通常该凝胶的比例为50%,甚至60%)。这就限制了使用范围,配制人员也会受到产品结构和触感的限制。另一缺点来自于后序试验:很难防止所得的产品被特殊的霉菌(例如,黑曲霉)污染,该细菌生长几乎不需要游离水,因此它对凝胶的失水作用的敏感度较低。French patent 2682296 proposes a non-chemical antiseptic method, the main feature of which is the use of glycerol-based poly(meth)acrylate gel, which is characterized by a strong penetrating effect on the environment, so that the cosmetic preparations can be dehydrated by dehydration. inactivation of microorganisms. Microbial contamination test (for example, on a cream containing 40% of the gel in question without chemical preservatives, inoculate 106 bacteria per gram of cream, control inoculation only in the presence of gel in the formulation 7 days) can illustrate the antimicrobial efficacy of the gel. The method described in this patent has proven to be practicable, but there are some disadvantages: the amount of gel required for the cosmetic composition is high (at least 40% in the best case; usually the proportion of this gel is 50%, even 60%). This limits the scope of use, and the formulator is limited by the structure and feel of the product. Another disadvantage stems from subsequent testing: it is difficult to prevent the resulting product from being contaminated by specific molds (e.g. Aspergillus niger), which requires little free water for growth and is therefore less sensitive to the dehydration effect of the gel .
本发明的目的是提供一种能增进化妆品防腐功效的凝胶,特别是能防止霉菌的生长,即一种具有改进的渗透性的凝胶。The object of the present invention is to provide a gel which improves the preservative efficacy of cosmetics, in particular against the growth of molds, ie a gel which has improved permeability.
本发明的另一目的是提供一种具有改进的化妆品特性、特别是触感的凝胶。Another object of the present invention is to provide a gel with improved cosmetic properties, especially feel.
本发明的另一目的是提供一种具有物理活性并具有抗菌功效的凝胶,它在化妆品组合物中的比例小于或等于20%。Another object of the present invention is to provide a gel with physical activity and antimicrobial efficacy, the proportion of which in the cosmetic composition is less than or equal to 20%.
本发明的目的是一种可用于化妆品或皮肤用药的具有抗微生物物理活性的凝胶,它包含至少一种多元醇和至少一种(甲基)丙烯酸聚合物,其特征在于还包含至少一种通式(1)所示的液化溶剂,并且所得产品中凝胶的比例约为1-20%,R1-O-(R2-O-R2)n-OR3 (1)其中R1是氢原子或C1-C5直链或支链烷基,R2是C1-C5直链或支链烷基,R3是氢原子或C1-C5直链或支链烷基,n是1-200000的整数。The object of the present invention is a gel with antimicrobial physical activity that can be used in cosmetics or dermopharmaceuticals, comprising at least one polyol and at least one (meth)acrylic polymer, characterized in that it also contains at least one The liquefaction solvent shown in formula (1), and the proportion of gel in the obtained product is about 1-20%, R 1 -O-(R 2 -OR 2 ) n -OR 3 (1) wherein R 1 is a hydrogen atom Or C 1 -C 5 straight chain or branched chain alkyl, R 2 is C 1 -C 5 straight chain or branched chain alkyl, R 3 is a hydrogen atom or C 1 -C 5 straight chain or branched chain alkyl, n It is an integer of 1-200000.
关于其它特征:-各多元醇的通式a,b,…i…-(烷基)-多元-醇其中:*烷基是Cn直链或支链烷基,n为2-10。*多元是醇官能团的数目。*a,b,…i表示1-10的不同数目,与醇官能团的取代位置相对应;-优选R1是C1-C3烷基,并且n是1-3。-凝胶中液化溶剂的比例为5-50%,优选15-30%;-聚合物衍生自丙烯酸和/或甲基丙烯酸,并且呈其盐、酯、酰胺的形式;-凝胶中聚合物的比例为0.05-5%,并且优选为0.2-1%;-凝胶中多元醇的比例为1-99%,并且优选为30-70%;-多元醇由30-50%的甘油和2-8%的1,2-辛二醇构成。-所得产品中凝胶的比例优选为5-20%。Regarding other characteristics: - the general formula a, b, ... i ... -(alkyl)-poly-alcohol for each polyol wherein: * Alkyl is C n linear or branched chain alkyl, n is 2-10. * Plity is the number of alcohol functional groups. * a, b, ...i represent different numbers from 1-10, corresponding to the substitution positions of the alcohol functional groups; - preferably R 1 is C 1 -C 3 alkyl, and n is 1-3. - the proportion of liquefaction solvent in the gel is 5-50%, preferably 15-30%; - the polymer is derived from acrylic acid and/or methacrylic acid and is in the form of its salts, esters, amides; - the polymer in the gel The proportion of polyol is 0.05-5%, and preferably 0.2-1%; - the proportion of polyol in the gel is 1-99%, and preferably 30-70%; - polyol is composed of 30-50% glycerol and 2 - 8% composition of 1,2-octanediol. - The proportion of gel in the resulting product is preferably 5-20%.
由于上述凝胶的物理抗菌活性,本发明的目的还在于将该凝胶用于化妆品或皮肤用药的防腐处理。Due to the physical antibacterial activity of the above-mentioned gel, the object of the present invention is also to use this gel for the preservative treatment of cosmetics or dermopharmaceuticals.
通过以下含各种组分的凝胶的非限定性实例来说明本发明,该凝胶本身由多元醇、聚(甲基)丙烯酸酯类聚合物、液化溶剂和水构成。The invention is illustrated by the following non-limiting example of a gel of various components, which itself consists of a polyol, a poly(meth)acrylate polymer, a liquefaction solvent and water.
多元醇的通式为:a,b,…i…-(烷基)-多元-醇其实例可为:-丙二醇(a=1,b=2,n=3)-1,3丁二醇(a=1,b=3,n=4)-甘油(a=1,b=2,c=3,n=3)-1,2-戊二醇(a=1,b=2,n=5)-1,2-辛二醇(a=1,b=2,n=8)-1,8-辛二醇(a=1,b=8,n=8)-甘露醇或山梨醇(a=1,b=2,c=3,d=4,e=5,f=6,n=6)-2-乙基-1,3-己二醇(a=1,b=2,n=8,支链)The general formula of polyols is: a, b, ... i...-(alkyl)-poly-alcohols, examples of which can be: -propylene glycol (a=1, b=2, n=3)-1,3 butanediol (a=1, b=3, n=4)-glycerol (a=1, b=2, c=3, n=3)-1,2-pentanediol (a=1, b=2, n =5)-1,2-octanediol (a=1, b=2, n=8)-1,8-octanediol (a=1, b=8, n=8)-mannitol or sorbitol Alcohol (a=1, b=2, c=3, d=4, e=5, f=6, n=6)-2-ethyl-1,3-hexanediol (a=1, b= 2, n=8, branched)
多元醇优选是含有高含量甘油的混合物。在特别优选的混合物中,凝胶中甘油的比例为30-50%,凝胶中1,2-辛二醇的比例为2-8%。The polyol is preferably a mixture with a high content of glycerol. In a particularly preferred mixture, the proportion of glycerol in the gel is 30-50%, and the proportion of 1,2-octanediol in the gel is 2-8%.
将甘油与其它多元醇混合可改进组合物的触感、可配制性,并能增进凝胶的渗透作用,即它吸收游离水的能力,也代表其抗微生物功效。Combining glycerin with other polyols improves the feel of the composition, formulatability, and increases the penetration of the gel, ie its ability to absorb free water, which also represents its antimicrobial efficacy.
聚合物优选自丙烯酸和/或甲基丙烯酸的钠盐、钾盐、三乙胺盐、三乙醇胺盐、铵盐,但也可选自这些酸性聚合物的酯或酰胺,或选自聚羧乙烯制剂型交联衍生物-例如由季戊四醇、蔗糖或丙烯的烯丙基醚交联而成。The polymer is preferably selected from the sodium, potassium, triethylamine, triethanolamine, ammonium salts of acrylic acid and/or methacrylic acid, but can also be selected from the esters or amides of these acidic polymers, or from carbopol Formulation-type cross-linked derivatives - such as pentaerythritol, sucrose or allyl ethers of propylene cross-linked.
凝胶中聚合物的比例为0.05-5%,优选为0.2-1%。The proportion of polymer in the gel is 0.05-5%, preferably 0.2-1%.
液化溶剂优选自醚,如甲氧基二甘醇、乙氧基二甘醇(或二甘醇单乙醚),丙氧基二甘醇、丁氧基二甘醇、三甘醇单丙基醚,或它们的酯,例如乙酸乙氧基二甘醇酯,或乙酸乙氧基乙酯。液化溶剂还可选自聚乙二醇或聚丙二醇,聚合度可达200000。这些溶剂有利地以混合物的形式被使用。The liquefaction solvent is preferably selected from ethers, such as methoxydiethylene glycol, ethoxydiethylene glycol (or diethylene glycol monoethyl ether), propoxydiethylene glycol, butoxydiethylene glycol, triethylene glycol monopropyl ether , or their esters, such as ethoxydiethylene glycol acetate, or ethoxyethyl acetate. The liquefaction solvent can also be selected from polyethylene glycol or polypropylene glycol, and the degree of polymerization can reach 200,000. These solvents are advantageously used in the form of a mixture.
本发明的凝胶实例可由以下组分制成:-40%甘油和6%1,2-辛二醇,-0.7%聚丙烯酸钠,-20%乙氧基二甘醇。An example of a gel according to the invention can be made from the following components: - 40% glycerin and 6% 1,2-octanediol, - 0.7% sodium polyacrylate, - 20% ethoxydiglycol.
剩余的是水,或包含33.3%的水。The rest is water, or contains 33.3% water.
本发明的凝胶在所得产品中的比例为1-99%,但优选为5-20%。The proportion of the gel of the invention in the resulting product is 1-99%, but preferably 5-20%.
本发明的凝胶适用于各种需要进行抗微生物防腐处理的用于化妆品的盖伦制剂:水包油型乳化体、油包水型乳化体、乳液、洗剂、凝胶、膏霜、净发剂、香波、护发素、皂类,这里所列举的不是限定性的。The gel of the present invention is applicable to various galenic preparations for cosmetics that require antimicrobial antiseptic treatment: oil-in-water emulsion, water-in-oil emulsion, emulsion, lotion, gel, cream, cleansing agent, etc. Hair lotion, shampoo, conditioner, soap, the list here is not limiting.
本发明的凝胶还可与包含其它常用的化妆品成分的化妆品组合物结合使用,这些成分有:提取或合成脂类、成胶聚合物和用于增加粘度的聚合物、表面活性剂和乳化剂、水溶性或油溶性活性成分、植物提取物、组织提取物、海洋生物提取物。The gels of the present invention can also be used in combination with cosmetic compositions comprising other usual cosmetic ingredients: extracted or synthetic lipids, gel-forming and viscosity-increasing polymers, surfactants and emulsifiers , water-soluble or oil-soluble active ingredients, plant extracts, tissue extracts, marine biological extracts.
包含本发明凝胶的化妆品组合物可用于调理或护理皮肤、头发、指甲和头皮,即进行抗老化、抗皱、抗炎、抗痤疮、防晒和抗自由基、滋润和润滑作用、防脱发、防止污染和侵害处理。Cosmetic compositions comprising the gel of the invention can be used for conditioning or caring for the skin, hair, nails and scalp, i.e. for anti-aging, anti-wrinkle, anti-inflammatory, anti-acne, sun protection and anti-free radical, moisturizing and lubricating effects, anti-hair loss, prevention of Pollution and infringement treatment.
本发明的凝胶特别适用于那些用于敏感、易受刺激皮肤的化妆品和皮肤用药,因此将它们归入那些称为“低刺激”或“柔和”产品,例如它们具有抗刺激的特性。The gels of the present invention are particularly suitable for use in those cosmetic and dermopharmaceutical applications for sensitive, irritated skin, whereupon they are classified as "low irritation" or "mild" products, eg they have anti-irritant properties.
这些凝胶的功效基于物理作用(渗透作用)。从而配制其中不含化学防腐剂的目的产物。The efficacy of these gels is based on physical action (osmosis). The desired product is thereby formulated without chemical preservatives.
Claims (10)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR95/09512 | 1995-08-04 | ||
| FR9509512A FR2737406B1 (en) | 1995-08-04 | 1995-08-04 | PHYSICAL ACTIVITY GEL FOR COSMETIC PRODUCTS |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1195284A true CN1195284A (en) | 1998-10-07 |
| CN1153565C CN1153565C (en) | 2004-06-16 |
Family
ID=9481719
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB961967331A Expired - Fee Related CN1153565C (en) | 1995-08-04 | 1996-08-02 | Physically active antimicrobial gel for cosmetic products |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US5891428A (en) |
| EP (1) | EP0841897B2 (en) |
| JP (1) | JPH11510176A (en) |
| KR (1) | KR19990036112A (en) |
| CN (1) | CN1153565C (en) |
| AT (1) | ATE201325T1 (en) |
| AU (1) | AU705817B2 (en) |
| CA (1) | CA2228731C (en) |
| DE (1) | DE69612982T3 (en) |
| ES (1) | ES2157455T5 (en) |
| FR (1) | FR2737406B1 (en) |
| WO (1) | WO1997005856A1 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116033909A (en) * | 2020-06-22 | 2023-04-28 | 信山科艺有限公司 | antibacterial composition |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH09143044A (en) * | 1995-11-17 | 1997-06-03 | White Lilly:Kk | Basic cosmetic without containing antimicrobial agent and germicide |
| DE19702092C2 (en) * | 1997-01-22 | 2002-01-17 | Cognis Deutschland Gmbh | Use of 1,2-alkanediols |
| FR2767697B1 (en) * | 1997-09-01 | 2000-05-05 | Boots Co Plc | DERMATOLOGICAL COMPOSITION FOR PREVENTING THE APPEARANCE OF SKIN HYPERSENSITIVITY AND INTOLERANCE SYMPTOMS |
| FR2768925B1 (en) * | 1997-09-29 | 1999-11-05 | Sederma Sa | COMPOSITIONS FOR COSMETIC OR DERMOPHARMACEUTICAL USE ACTIVE AGAINST MULTIPLE CHEMICAL AGGRESSIONS ON THE SKIN |
| US20030039580A1 (en) * | 2001-02-26 | 2003-02-27 | Lonza Inc. | Stable preservative formulations comprising halopropynyl compounds and butoxydiglycol solvent |
| JP3696837B2 (en) * | 2002-02-04 | 2005-09-21 | 株式会社資生堂 | Fragrance composition |
| DE10206759A1 (en) | 2002-02-19 | 2003-08-28 | Dragoco Gerberding Co Ag | Use of 1,2-alkanediol mixture as an antimicrobial agent, e.g. for treating body odor, acne or mycoses or preserving perishable products |
| US7053029B2 (en) * | 2002-03-27 | 2006-05-30 | Kimberly-Clark Worldwide, Inc. | Use indicating soap |
| US7960326B2 (en) * | 2002-09-05 | 2011-06-14 | Kimberly-Clark Worldwide, Inc. | Extruded cleansing product |
| CA2492976C (en) * | 2002-09-05 | 2011-11-01 | Galderma Research & Development, S.N.C. | Solution for ungual and peri-ungual application |
| FR2844197B1 (en) * | 2002-09-05 | 2006-06-23 | Galderma Res & Dev | SOLUTION FOR UNIGEAL AND PERI-UNGEAL APPLICATION |
| ES2381359T3 (en) | 2003-11-17 | 2012-05-25 | Sederma | Compositions containing mixtures of tetrapeptides and tripeptides |
| FR2880802B1 (en) | 2005-01-14 | 2008-12-19 | Sederma Soc Par Actions Simpli | COSMETIC OR DERMOPHARMACEUTICAL COMPOSITION CONTAINING EUGLENE EXTRACT |
| JP2006232732A (en) * | 2005-02-25 | 2006-09-07 | Shiseido Co Ltd | Emulsion composition |
| JP2006249049A (en) * | 2005-03-14 | 2006-09-21 | Shiseido Co Ltd | Skin care composition |
| FR2885522B1 (en) * | 2005-05-13 | 2020-01-10 | Sederma | COSMETIC OR DERMOPHARMACEUTICAL COMPOSITION CONTAINING TEPRENONE |
| FR2890310B1 (en) * | 2005-09-06 | 2009-04-03 | Sederma Soc Par Actions Simpli | USE OF PROTOBERBERINS AS AGENTS REGULATING THE ACTIVITY OF THE PILOSEBACEE UNIT |
| WO2007093839A1 (en) | 2006-02-16 | 2007-08-23 | Sederma | New polypeptides kxk and their use |
| FR2900573B1 (en) | 2006-05-05 | 2014-05-16 | Sederma Sa | NOVEL COSMETIC COMPOSITIONS COMPRISING AT LEAST ONE PEPTIDE CONTAINING AT LEAST ONE BLOCKED AROMATIC CYCLE |
| FR2939799B1 (en) | 2008-12-11 | 2011-03-11 | Sederma Sa | COSMETIC COMPOSITION COMPRISING ACETYL OLIGOGLUCURONANS. |
| FR2941231B1 (en) | 2009-01-16 | 2016-04-01 | Sederma Sa | NOVEL PEPTIDES, COMPOSITIONS COMPRISING THEM AND COSMETIC AND DERMO-PHARMACEUTICAL USES |
| FR2941232B1 (en) | 2009-01-16 | 2014-08-08 | Sederma Sa | NOVEL PEPTIDES, COMPOSITIONS COMPRISING THEM AND COSMETIC AND DERMO-PHARMACEUTICAL USES |
| WO2010082177A2 (en) | 2009-01-16 | 2010-07-22 | Sederma | New compounds, in particular peptides, compositions comprising them and cosmetic and dermopharmaceutical uses |
| FR2944435B1 (en) | 2009-04-17 | 2011-05-27 | Sederma Sa | COSMETIC COMPOSITION COMPRISING ORIDONIN |
| FR2945939B1 (en) | 2009-05-26 | 2011-07-15 | Sederma Sa | COSMETIC USE OF TYR-ARG DIPEPTIDE TO FIGHT SKIN RELEASE. |
| FR2973701B1 (en) | 2011-04-06 | 2013-10-04 | Biopass S A | COMPOSITION FOR TOPICAL APPLICATION |
| FR2997299B1 (en) | 2012-10-30 | 2014-12-26 | Sederma Sa | ASSOCIATION OF PLANT EXTRACTS, COSMETIC ACTIVE INGREDIENT AND COMPOSITION CONTAINING THE SAME, AND COSMETIC TOPICAL USE |
| FR3007014B1 (en) * | 2013-06-18 | 2016-02-05 | Dior Christian Parfums | METHOD AND DEVICE FOR FILLING A UNITARY CONTAINER FROM A CAPSULE, AND CAPSULE USES THEREFOR |
| FR3024037B1 (en) | 2014-07-25 | 2018-03-02 | Sederma | COSMETIC OR DERMATOLOGICAL ACTIVE INGREDIENT COMPRISING A MIXTURE OF UNSATURATED FATTY DICARBOXYLIC ACIDS, COMPOSITIONS COMPRISING THE SAME, AND COSMETIC OR DERMATOLOGICAL USES |
| WO2021259215A1 (en) | 2020-06-22 | 2021-12-30 | Rht Limited | Antiseptic compositions |
| FR3162143A1 (en) * | 2024-05-20 | 2025-11-21 | Cosmosoft | Hydrogel, cosmetic composition, container and preparation process |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2491933B1 (en) * | 1980-10-10 | 1985-07-12 | Oreal | NOVEL POLYETHYLENE GLYCOLS DERIVATIVES, THEIR USE AND COSMETIC AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
| US5114717A (en) * | 1991-02-08 | 1992-05-19 | Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. | Clear cosmetic sticks with compatible fragrance components |
| FR2682296B1 (en) * | 1991-10-14 | 1993-11-12 | Sederma Sa | NOVEL COSMETIC COMPOSITIONS CONTAINING POLYMERIC GELS. |
| US5437867A (en) * | 1993-03-19 | 1995-08-01 | Collaborative Laboratories | Solubilizing, thickening and emulsifying cosmetic composition and process for preparation of same |
| CA2177682C (en) * | 1993-12-23 | 1999-12-28 | Sekhar Mitra | Antimicrobial wipe compositions |
| AU2638795A (en) † | 1994-06-17 | 1996-01-15 | University Of Nebraska Board Of Regents | In situ gel-forming delivery vehicle for bio-affecting substances, and method of use |
-
1995
- 1995-08-04 FR FR9509512A patent/FR2737406B1/en not_active Expired - Lifetime
-
1996
- 1996-08-02 JP JP9508172A patent/JPH11510176A/en not_active Ceased
- 1996-08-02 DE DE69612982T patent/DE69612982T3/en not_active Expired - Lifetime
- 1996-08-02 AT AT96927728T patent/ATE201325T1/en not_active IP Right Cessation
- 1996-08-02 CA CA2228731A patent/CA2228731C/en not_active Expired - Lifetime
- 1996-08-02 US US09/011,057 patent/US5891428A/en not_active Expired - Lifetime
- 1996-08-02 CN CNB961967331A patent/CN1153565C/en not_active Expired - Fee Related
- 1996-08-02 KR KR1019980700780A patent/KR19990036112A/en not_active Withdrawn
- 1996-08-02 EP EP96927728A patent/EP0841897B2/en not_active Expired - Lifetime
- 1996-08-02 AU AU67443/96A patent/AU705817B2/en not_active Ceased
- 1996-08-02 WO PCT/FR1996/001229 patent/WO1997005856A1/en not_active Ceased
- 1996-08-02 ES ES96927728T patent/ES2157455T5/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116033909A (en) * | 2020-06-22 | 2023-04-28 | 信山科艺有限公司 | antibacterial composition |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0841897B1 (en) | 2001-05-23 |
| CN1153565C (en) | 2004-06-16 |
| EP0841897A1 (en) | 1998-05-20 |
| DE69612982T3 (en) | 2004-11-11 |
| ES2157455T5 (en) | 2004-12-01 |
| KR19990036112A (en) | 1999-05-25 |
| ES2157455T3 (en) | 2001-08-16 |
| JPH11510176A (en) | 1999-09-07 |
| CA2228731C (en) | 2010-11-16 |
| FR2737406B1 (en) | 1997-10-24 |
| AU705817B2 (en) | 1999-06-03 |
| AU6744396A (en) | 1997-03-05 |
| FR2737406A1 (en) | 1997-02-07 |
| DE69612982D1 (en) | 2001-06-28 |
| DE69612982T2 (en) | 2001-09-13 |
| CA2228731A1 (en) | 1997-02-20 |
| EP0841897B2 (en) | 2004-06-30 |
| US5891428A (en) | 1999-04-06 |
| WO1997005856A1 (en) | 1997-02-20 |
| ATE201325T1 (en) | 2001-06-15 |
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